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558 results for “austria”
FIGURE 2 in New taxonomic, stratigraphic, and geographic information on the genus Faksephyllia Floris, 1972 (Scleractinia; Caryophylliidae); first records from the Oligocene of Austria, Germany, and Italy
FIGURE 2. Map showing the distribution of Faksephyllia in the Oligocene and one possible occurrence in the Eocene (from north to south, marked by Δ): Oligocene of Germany (Reit im Winkel, Bavaria), Austria (Tyrol), Italy (Vicenza area). Possible Eocene occurrence: Bosnia-Herzegovina (Rošići area).
FIGURES 11–14. 11 in Notes on Acanthoderini (Coleoptera, Cerambycidae, Lamiinae) described by Ernst Fuchs, now in the Herbert Schmid Collection, Vienna, Austria
FIGURES 11–14. 11, Psapharochrus plaumanni (Fuchs), holotype male; 12, Psapharochrus pseudopropinquus (Fuchs), holotype female; 13, Acanthoderes sexmaculatus Fuchs, holotype female = Psapharochrus schmithi (Melzer); 14, Oreodera ferruginea Fuchs, holotype female = Sorelia cervina Lane.
FIGURE 1 in Two new dragonflies (Odonata: Anisoptera) from the Miocene of Carinthia (Austria)
FIGURE 1. Photograph of the hind wing fragment of Ictinogomphus hassleri sp. nov., holotype LMK-Pal-2016-5538.
FIGURE 4 in Two new dragonflies (Odonata: Anisoptera) from the Miocene of Carinthia (Austria)
FIGURE 4. Photograph of the hind wing fragment of Gomphaeschna carinthiae sp. nov., holotype UMJG&P 211472, plate B. The posterobasal area of the wing is covered with sediment.
FIGURE 3 in Two new dragonflies (Odonata: Anisoptera) from the Miocene of Carinthia (Austria)
FIGURE 3. Photograph of the hind wing fragment of Gomphaeschna carinthiae sp. nov., holotype UMJG&P 211472, plate A. The wingtip is covered with sediment.
FIGURE 5 in Two new dragonflies (Odonata: Anisoptera) from the Miocene of Carinthia (Austria)
FIGURE 5. Drawing of the hind wing fragment of Gomphaeschna carinthiae sp. nov., holotype UMJG&P 211472. The drawing involves features of both plates.
FIGURE 2 in Two new dragonflies (Odonata: Anisoptera) from the Miocene of Carinthia (Austria)
FIGURE 2. Drawing of the hind wing fragment of Ictinogomphus hassleri sp. nov., holotype LMK-Pal-2016-5538, with terminology of wing venation.
Austria Synthetic Ecosystem
Austria synthetic ecosystem dataset consisting of tables for persons and households. This dataset was created by the SPEW R Package using the following input data sources: GeoHive counts and IPUMS-I shapefiles and microdata.
FIGURE 13. A in Diplocephalus komposchi n. sp., a new species of erigonine spider (Araneae, Linyphiidae) from Austria
FIGURE 13. A, Geographic position of the type locality (black dot) of Diplocephalus komposchi n. sp. in Austria (AT) at the border to Slovenia (SI). B, Locality of Diplocephalus komposchi n. sp. in the "Petzen" area; view from the "Kniepssattel" towards WNW showing the peaks "Knieps" and "Feistritzer Spitz" [Photo: Christian Komposch, 8 September 2009].
FIGURES 1–8. Diplocephalus komposchi n in Diplocephalus komposchi n. sp., a new species of erigonine spider (Araneae, Linyphiidae) from Austria
FIGURES 1–8. Diplocephalus komposchi n. sp. 1–3, Female allotype; 4–8, male holotype. 1, Female prosoma lateral. 2, Epigynum, ventral. 3, Epigynum, dorsal. 4, Male prosoma, lateral. 5, Ditto, dorsal. 6, Male tibia, dorsal. 7, Expanded male palp. 8, Embolic division, distal. Scale bars, 1, 4, 0.5 mm; 2–3, 0.2 mm; 5, 0.5 mm; 6–7, 0.25 mm; 8, 0.1 mm.
FIGURES 9–12 in Diplocephalus komposchi n. sp., a new species of erigonine spider (Araneae, Linyphiidae) from Austria
FIGURES 9–12. Micro-computed tomographic (MCT) images of the dissected palp of Diplocephalus komposchi n. sp. 9, Male paratype. 10, Tegulum and subtegular division and embolic division combined. 11, Embolic division. 12, Tegulum and subtegular division. Scale bars, 9, 0.1 mm; 10–12, 0.1 mm.
Austria Nightlights
Nighttime lights in Austria available in raster format as yearly values from 1992 to 2013. Nightlights are expressed as Digital Number (DN) values, ranging from 0 (no luminosity) to 63 (maximum luminosity). Nightlights data are ready-to-use (i.e. intercalibration of original satellite values to allow for temporal comparison and average of simultaneous satellite already performed).
Population of Austria since 1981
<p>Dataset containing absolute population numbers for male/female inhabitants of Austria</p>
Statistics of population in Upper Austria
<p>The result of the experiment 'Statistics of population in Upper Austria'.</p> <p>Contains a database dump of a Postgres version 9.5.2</p> <p>Metadata can be obtained here: https://www.data.gv.at/katalog/dataset/e108dcc3-1304-4076-8619-f2185c37ef81</p> <p>The population table contains the data from the Link but filtered. Only the following columns are available. The metadata of the columns are the same as in the link above.</p> <ul> <li>lau2_code </li> <li>lau2_name </li> <li>year </li> <li>sex </li> <li>age_total</li> </ul> <p>In the calculation table the result is stored. The following columns exists:</p> <ul> <li>year </li> <li>sex </li> <li>mean</li> </ul> <p>'Year' is the year when the data was observed. </p> <p>'Sex' represents the gender of the population and can have the values 0,1,2 (1 = male, 2 = female, 0 = total)</p> <p>'mean' is the average population per village.</p> <p> </p>
Silver coin of Austria (1630).
Silver coin of Austria (1630). Monetary unit: thaler. Denomination: 1. Year of issue: 1630. Material: silver. Серебряная монета Австрии (1630). Денежная единица: талер. Номинал: 1. Год выпуска: 1630. Материал: серебро. Source: Objaverse 1.0 / Sketchfab
In situ limnological measurements collected in Lake Mondsee (Austria) from 1998 to 2017
<p><span>Two detailed datasets, including Photosynthetically Active Radiation (PAR) records and water column profiles of several standard parameters obtained by multi-parameter sonde measurements during monthly surveys. These datasets may serve as references for future comparisons of critical water body features under changing environmental conditions in Lake Mondsee and elsewhere.</span></p>
Netzero2040: Reaching climate neutrality in Austria by 2040: engaging stakeholders for model-supported scenario development. Data repository
<p><span>This repository contains scenario results in pyam format, qualitative scenario narratives and drivers identified by stakeholders for the NetZero2040 project.</span></p> <p><span>NetZero2040 developed the first independent scenarios achieving climate-neutrality in Austria by 2040. We improve on previous analyses by employing a structured co-creation process involving stakeholders and modellers, simultaneously modelling the whole energy system and the electricity system in great detail, creating shared visions of a climate-neutral future. Results are openly available and have been broadly disseminated in the scientific community and to the public. Our scenarios are differentiated by assumptions on energy demand and imports of energy carriers. They show that a rapid electrification of transport and heating, in combination with a build out rate of renewable energies which is well above historical maxima in the Austrian power system, allow significant emission reductions until 2030, and that these measures are consistently required in all scenarios. However, after 2030 scenarios diverge and uncertainty about the most cost-efficient transformation measures prevail. </span></p>
Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W & SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C & S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland. in Canidae
Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W & SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C & S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland.
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina. in Canidae
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina.
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.